510(k) K032058 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
MODIFICATION TO REPROCESSED SYNTHES EXTERNAL FIXATION DEVICES
| Applicant | Alliance Medical Corp., Phoenix AZ, US |
| Decision | Substantially Equivalent, Jul 30, 2003 |
| Received | Jul 2, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032058
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.